Amelogenesis Imperfecta encompasses a range of diverse conditions characterized by structural defects in tooth enamel development, featuring intricate inheritance patterns. These conditions can manifest in both primary and permanent dentition and may be inherited through autosomal dominant, autosomal recessive, or X-linked modes of transmission. The treatment plan involves considering various factors including the patient's age, the nature and extent of the disorder, intraoral factors, and the patient's socioeconomic status. In this report, we present cases of two siblings diagnosed with hypoplastic amelogenesis imperfecta through clinical and radiographic assessments.

Keywords : Amelogenesis, Amelogenesis Imperfecta, Enamel hypoplasia